Evidence map›Paper›PMID 30733541›Full record

ArticleScientific reports2019

MD001, a Novel Peroxisome Proliferator-activated Receptor α/γ Agonist, Improves Glucose and Lipid Metabolism.

Seok-Ho Kim, Shin Hee Hong, Young-Joon Park, Jong-Hyuk Sung, Wonhee Suh, Kyeong Won Lee, Kiwon Jung, Changjin Lim, Jin-Hee Kim, Hyoungsu Kim and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Seok-Ho KimDepartment of Pharmacy, College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Pocheon, Gyeonggi-do, 11160, Korea.
Shin Hee HongCollege of Pharmacy, Ajou University, Suwon, Gyeonggi-do, 16499, Korea.
Young-Joon ParkCollege of Pharmacy, Ajou University, Suwon, Gyeonggi-do, 16499, Korea.
Jong-Hyuk SungCollege of Pharmacy, Yonsei University, Songdo, Incheon, 405-750, Korea.
Wonhee SuhCollege of Pharmacy, Chung-Ang University, Seoul, 156-756, Korea.
Kyeong Won LeeMarine Biotechnology Research Center, Korea Institute of Ocean Science & Technology 787 Haeanlo, Ansan, Gyeonggi-do, 426-744, Korea.
Kiwon JungDepartment of Pharmacy, College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Pocheon, Gyeonggi-do, 11160, Korea.
Changjin LimDepartment of Pharmacy, College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Pocheon, Gyeonggi-do, 11160, Korea.
Jin-Hee KimCollege of Pharmacy, Yonsei University, Songdo, Incheon, 405-750, Korea.
Hyoungsu KimCollege of Pharmacy, Ajou University, Suwon, Gyeonggi-do, 16499, Korea.
Kyong Soo ParkThe Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul National University College of Medicine, Seoul, 03080, Korea.ORCID 0000-0003-3597-342X
Sang Gyu ParkCollege of Pharmacy, Ajou University, Suwon, Gyeonggi-do, 16499, Korea. sgpark@ajou.ac.kr.ORCID 0000-0002-4870-2242
Ajou University · KRCHA University · KRYonsei University · KRChung-Ang University · KRKorea Institute of Ocean Science and Technology · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peroxisome proliferator-activated receptor (PPAR)-α/γ dual agonists have been developed to treat metabolic diseases; however, most of them exhibit side effects such as body weight gain and oedema. Therefore, we developed a novel PPARα/γ dual agonist that modulates glucose and lipid metabolism without adverse effects. We synthesised novel compounds composed of coumarine and chalcone, determined their crystal structures, and then examined their binding affinity toward PPARα/γ. We investigated the expression of PPARα and PPARγ target genes by chemicals in HepG2, differentiated 3T3-L1, and C2C12 cells. We examined the effect of chemicals on glucose and lipid metabolism in db/db mice. Only MD001 functions as a PPARα/γ dual agonist in vitro. MD001 increased the transcriptional activity of PPARα and PPARγ, resulting in enhanced expression of genes related to β-oxidation and fatty acid and glucose uptake. MD001 significantly improved blood metabolic parameters, including triglycerides, free fatty acids, and glucose, in db/db mice. In addition, MD001 ameliorated hepatic steatosis by stimulating β-oxidation in vitro and in vivo. Our results demonstrated the beneficial effects of the novel compound MD001 on glucose and lipid metabolism as a PPARα/γ dual agonist. Consequently, MD001 may show potential as a novel drug candidate for the treatment of metabolic disorders.

Indexed as

AnimalsChalconesCoumarinsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2GlucoseHEK293 CellsHep G2 CellsHumansHypoglycemic AgentsInsulin ResistanceLipid MetabolismMaleMiceMice, Inbred C57BLPPAR alphaChalconesCoumarinsGlucoseHypoglycemic Agentsinterruptin BPPAR alphaPPAR gamma

Identifiers

PMID30733541
PMCPMC6367362
OpenAlexW2914581091

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.